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3DEN

Structure of E. coli DHDPS mutant Y107W

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0008652biological_processamino acid biosynthetic process
A0008840molecular_function4-hydroxy-tetrahydrodipicolinate synthase activity
A0009085biological_processlysine biosynthetic process
A0009089biological_processlysine biosynthetic process via diaminopimelate
A0016829molecular_functionlyase activity
A0019752biological_processcarboxylic acid metabolic process
A0019877biological_processdiaminopimelate biosynthetic process
A0042802molecular_functionidentical protein binding
B0003824molecular_functioncatalytic activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0008652biological_processamino acid biosynthetic process
B0008840molecular_function4-hydroxy-tetrahydrodipicolinate synthase activity
B0009085biological_processlysine biosynthetic process
B0009089biological_processlysine biosynthetic process via diaminopimelate
B0016829molecular_functionlyase activity
B0019752biological_processcarboxylic acid metabolic process
B0019877biological_processdiaminopimelate biosynthetic process
B0042802molecular_functionidentical protein binding
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K A 293
ChainResidue
AALA152
AVAL154
ALYS155
AILE157
AHOH501

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 294
ChainResidue
AASP29
AALA33
AHIS125
AGOL295

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 295
ChainResidue
ALYS26
ATYR30
AHIS125
AGOL294

site_idAC4
Number of Residues1
DetailsBINDING SITE FOR RESIDUE PO4 A 296
ChainResidue
AARG109

site_idAC5
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A2647
ChainResidue
AALA81
AGLU84
AHOH312
AHOH439
AHOH440
BALA49
BTHR50
BLEU51
BASN52

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE K B 293
ChainResidue
BALA152
BVAL154
BLYS155
BILE157

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PO4 B 294
ChainResidue
AHOH523
BARG21
BLYS25
BHOH356

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PO4 B 295
ChainResidue
BTYR116
BLYS120
BARG150
BHOH432
BHOH449

Functional Information from PROSITE/UniProt
site_idPS00665
Number of Residues18
DetailsDHDPS_1 Dihydrodipicolinate synthase signature 1. AIVsvGTTGESatlnhdE
ChainResidueDetails
AALA38-GLU55

site_idPS00666
Number of Residues31
DetailsDHDPS_2 Dihydrodipicolinate synthase signature 2. YNVPsrTgcdLlpetvgrlakvkn.IiGIKEA
ChainResidueDetails
ATYR133-ALA163

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsActive site: {"description":"Proton donor/acceptor"}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues2
DetailsActive site: {"description":"Schiff-base intermediate with substrate"}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_00418","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"20353808","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"22552955","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsSite: {"description":"Part of a proton relay during catalysis"}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues2
DetailsSite: {"description":"L-lysine inhibitor binding; via carbonyl oxygen"}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues6
DetailsSite: {"description":"L-lysine inhibitor binding"}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dhp
ChainResidueDetails
AARG138
ATYR133

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dhp
ChainResidueDetails
BARG138
BTYR133

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dhp
ChainResidueDetails
ATHR44
ATHR45

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dhp
ChainResidueDetails
BTHR44
BTHR45

site_idMCSA1
Number of Residues6
DetailsM-CSA 267
ChainResidueDetails
ATHR44hydrogen bond acceptor, hydrogen bond donor
ATRP107hydrogen bond donor
ATYR133activator, electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor, proton relay
AARG138electrostatic stabiliser
AKGC161covalently attached, electron pair acceptor, electron pair donor, hydrogen bond acceptor, hydrogen bond donor, nucleofuge, nucleophile, proton acceptor, proton donor
AALA207activator, increase electrophilicity, polar interaction, steric role

site_idMCSA2
Number of Residues6
DetailsM-CSA 267
ChainResidueDetails
BTHR44hydrogen bond acceptor, hydrogen bond donor
BTRP107hydrogen bond donor
BTYR133activator, electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor, proton relay
BARG138electrostatic stabiliser
BKGC161covalently attached, electron pair acceptor, electron pair donor, hydrogen bond acceptor, hydrogen bond donor, nucleofuge, nucleophile, proton acceptor, proton donor
BALA207activator, increase electrophilicity, polar interaction, steric role

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PDB entries from 2025-12-24

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